510(k) Report

FDA applicant

Magnum Diamond, Inc.

San Antonio, TX2 decisions1985–19890 recalls

FDA records 2 decisions for Magnum Diamond, Inc. (San Antonio, TX) from 1985 to 1989: 2 510(k) clearances. Most are in product codes HNN (Knife, Ophthalmic) and GDM (Needle, Aspiration And Injection, Reusable). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Magnum Diamond, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magnum Diamond, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magnum Diamond, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • HNNKnife, Ophthalmic1decision
  • GDMNeedle, Aspiration And Injection, Reusable1decision

What has FDA decided for it lately?

  • K895752Diamond Blade Surgical KnivesMagnum Diamond, Inc. · 1989
  • K853499Micron-ScopeMagnum Diamond, Inc. · 1985

All 2 as Magnum Diamond, Inc. →

Other applicant names beginning “Magnum”

FDA records each applicant name separately; these may or may not be the same firm.

Magnum Instruments, Inc. 2Magnum Equipment LLC 1Magnum Health and Safety Pvt, Ltd. 1